Canonical Allele Identifier: PA2826094219
Gene: TYROBP HGNC NCBI

Linked Data

ClinVar Variation Id: 56394
ClinVar RCV Id: RCV000049807

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166985.1:p.Ser28Asn
CA263863
NM_001173514.2:c.83G>A